Average salary: £51,843 /yearly
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- £65k - £87k per annumEstimated...that expansion — from in-region setup to scaling day-to-day delivery. ~ A track record as the accountable lead on CE marking under EU MDR, or equivalent clearances in the EMEA regions. ~ Direct authority engagement — you've planned and led pre-submission and submission...SuggestedFull-timeLive-in
- £43k - £56k per annumEstimated...such as registration documentation and product applications and renewals to local authorities primarily focus on FDA 510(K) and UK/EU MDR. You will identify and maintain documentation including updates and review of the technical files for the IVF devices product portfolio...SuggestedFull-timeRemoteShift work
- £37k - £48k per annumEstimated...to the wider team. Working with Quality and Regulatory colleagues, support any commercial activity required to achieve and maintain MDR compliance across the Global Ostomy portfolio. Working with a wider group of stakeholders in the case of changes to pouches & accessories...SuggestedFull-time
- ...projects would be preferred. Managing budgets, produce scope of work and setting project objectives. Creating and maintaining Piping MDR Creating and implementing cost controls (Including Man-hour control), Monitor and manage team performance and their productivity....SuggestedPermanentFull-timeSelf-employedFreelanceFlexible hours
£60 - £75 per hour
...projects independently. Familiarity with global drug and device development processes, regulations, and guidelines (GxP, GCP, ICH, ISO, MDR/IVDR). Expertise in clinical and safety regulatory documentation throughout the product life cycle. Strong analytical skills with...SuggestedHourly payTemporaryHybrid workingRemoteRelocationFlexible hours- ...Technical Documentation · Develop and maintain Technical Documentation in line with ISO 13485, the Medical Device Regulation 2017/745 (EU MDR) and other applicable regulatory requirements. · Support the creation and review of labelling and marketing materials to ensure...SuggestedFull-timeOn-site
£35k - £45k per annum
...environments Knowledge of Hyper-V, VMware or other virtualisation platforms Exposure to cyber security technologies including SIEM and MDR solutions Experience working within ITIL or SLA-driven service environments Knowledge of backup and disaster recovery solutions The...SuggestedLong-term contractPermanentFull-timeOn-site- £28k - £38k per annumEstimated...manner, enabling rapid access by project team members and auditors. • Administer and maintain the project Master Document Register (MDR) and Drawing Register, keeping these up to date at all times and providing regular status reports to the Project Manager. • Manage the...Suggested
£60k - £80k per annum
...cybersecurity strategies, roadmaps, and investment recommendations. Position and sell cybersecurity solutions and services including MDR, SOC services, Microsoft Security solutions, Identity & Access Management, Cloud Security, Vulnerability Management, Security...SuggestedFull-timeField Solutions Group
Hertford, Hertfordshire9 days ago£50k - £68k per annum
...manufacturing or multi-site operational environments is desirable Familiarity with network security principles and integration with SOC or MDR services is desirable Exposure to network automation, scripting or infrastructure-as-code such as Python or Ansible is desirable...SuggestedFixed-term contractHybrid workingMonday to FridayBritish Steel
Scunthorpe, North Lincolnshire8 hours ago£90k per annum
...deals across mid-market and enterprise clients. Technical Breadth: Hands-on exposure across as many of the following as possible — MDR, SIEM, EDR, XDR, NDR, NGFW, IDS/IPS, WAF, SASE, SSE, NAC, PAM, MFA, SSO, DLP, SOAR, Threat Intelligence, Incident Response, CNAPP, CASB...SuggestedPermanent- £62k - £81k per annumEstimated...recognized technical expert in software quality, and Quality Management System (QMS) integration, ensuring alignment with ISO 13485 and EU MDR requirements while enabling modern software development practices. What you'll be doing: Lead and govern activities that ensure...SuggestedFull-time
- £44k - £57k per annumEstimated...Makes You Stand Out Independent ownership of PMS processes and documentation Strong working knowledge of global PMS regulations (EU MDR, FDA, ISO 14155) Advanced analytical skills, critical thinking and ability to interpret multi-source data Effective cross-...SuggestedFull-time
- £65k - £84k per annumEstimated...Engineering Lead for AI/ML Software, you will support the regulatory strategy for Neko’s AI- and ML-powered medical software, covering EU MDR, FDA, and UK MDR. You will collaborate closely with engineering, quality, and clinical teams, translating complex global requirements...SuggestedFull-time
- £53k - £70k per annumEstimated...Conduct cybersecurity maturity and risk assessment and for clients Practical experience implementing security controls, in areas such as MDR, IAM, Network Security, Cloud Deployments Advise clients on cybersecurity strategy, metrics and reporting for various levels of...SuggestedFlexible hours
- £48k - £64k per annumEstimated...What we look for Significant technical tax experience, including familiarity with current international developments (e.g., BEPS, MDR, operational tax changes including the EU FASTER initiative) An ability to work to tight deal deadlines Excellent relationship management...Long-term contractPermanentFlexible hours
- £40k - £52k per annumEstimated...ensure consistency of service standards nationally. Governance, Quality & Compliance Ensure compliance with ISO 13485, ISO 14001, MDR, Quality Management System (QMS) requirements and NHS site policies. Ensure field service documentation is accurate, audit-ready and...
- £57k - £72k per annumEstimated...providers as required per the SWICC supplier management program, in compliance with ISO 13485:2016 and other applicable regulations (e.g. EU MDR). • Develop and maintain the risk-based supplier qualification process, including quality questionnaires, desktop assessments, and on...Long-term contractFlexible hours
- £50k - £65k per annumEstimated...Risk Management application. IEC 62304: Comprehensive understanding of Software Lifecycle processes. (Good to have not a must) EU MDR Technical Documentation: Proven experience in preparing and maintaining documentation for regulatory compliance. How We Work We empower...Long-term contractFull-timeHybrid workingOn-siteRemoteFlexible hours
- £74k - £94k per annumEstimated...strategic planning and implementation of Regulatory and Quality Aspects of the business. Maintain a current expert knowledge of US FDA, EU MDR, and other applicable regulations, Legislations, best practices, and guidelines related to QA/RA, monitor changes to applicable laws...Full-timeShift workNight shift
- £43k - £56k per annumEstimated...& Experience Trained Internal Quality System Auditor and/or Software Quality Auditor. Experience with Medical Device Regulation (MDR) and MDSAP requirements. Knowledge of: ISO 27001, ISO 42001, NIST Cybersecurity Framework, FDA Pre-Market and Post-Market Cybersecurity...Full-timeHybrid working
- £63k - £83k per annumEstimated...or healthtech environment. Knowledge of medical device regulation and clinical software compliance across both EU and UK regimes (EU MDR/IVDR, and UKCA marking under the UK MDR 2002). Why Work for Proximie? ~ You will be encouraged to grow in your role, take ownership...PermanentFull-timeSummer workOn-siteFlexible hours
£30k - £35k per annum
...Reporting to the IT delivery Team Leader Setup and Installation of new Workstations / laptop devices. Rollout of Flotek security products, MDR, Email Threat Protection, Anti Virus solutions, Document / password management applications Assist in large scale email / data...PermanentFull-timeOn-siteMonday to FridayFlexible hours- £43k - £58k per annumEstimated...knowledge of Microsoft packages SharePoint, E-learning, TrackWise experience is desirable Knowledge in Medical device regulation (MDR, UKMDR), MDD and EUMDR is desirable Ability to work unsupervised / remotely Ability to work well with others across UK and...Remote
- £53k - £69k per annumEstimated...support OrganOx in maintaining compliance with ISO 13485, Code of Federal Regulations Title 21 parts 801, 806, 807, 820 under FDA QMSR, EU MDR 2017/745, UK Medical Device Regulations 2026, Canadian Medical Device Regulation SOR-98/282, Australian therapeutic Goods Act 1989,...Full-timeFlexible hours
- £22k - £26k per annumEstimated...Additional qualifications in Quality Management or Regulatory Affairs advantageous Knowledge of medical device and IVD regulations (EU MDR/IVDR, FDA, international requirements) Experience with regulatory submissions and documentation management Strong technical...Full-timeOn-siteMonday to Friday
- ...Estate’s marine strategy and public value ambitions. The role will lead the development and execution of engagement programs around the MDR, sector objectives, and leasing programs, coordinating strategic engagement activities, and working closely with internal colleagues...Flexible hours
- £33k - £43k per annumEstimated...Skills & Experience Knowledge of vulnerability management. Experience in dealing with cyber incidents. Basic knowledge of managing MDR, EDR and email security systems. Experience in assisting with Disaster Recovery and Business Continuity exercises. Strong...Hybrid workingOn-siteWork from home
£80k - £90k per annum
...systems and modern application platforms Oversee internal security monitoring and collaborate with external security partners (SOC/MDR) Lead incident and problem management activities, including root cause analysis and service restoration Leadership & Vendor Management...PermanentFull-time- £49k - £64k per annumEstimated...obtain and maintain market clearance or approval for medical devices in key global markets, with a primary focus on European Union EU MDR and United States FDA requirements. Prepare high-quality regulatory submissions, support compliance with applicable regulations, and...Full-timeNo agency
